ZENTEL

This brand name is authorized in Australia, Ecuador, France, Malta, Mexico, Nigeria, Poland, Romania, Singapore, South Africa.

Active ingredients

The drug ZENTEL contains one active pharmaceutical ingredient (API):

1
UNII F4216019LN - ALBENDAZOLE
 

Albendazole causes degenerative alterations in the tegument and intestinal cells of the worm by binding to the colchicine-sensitive site of tubulin, thus inhibiting its polymerization or assembly into microtubules.

 
Read more about Albendazole

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
P02CA03 Albendazole P Antiparasitic products, insecticides and repellents → P02 Anthelmintics → P02C Antinematodal agents → P02CA Benzimidazole derivatives
Discover more medicines within P02CA03

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
AU Pharmaceutical Benefits Scheme 8503M, 9047E
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 25.042-04-03, 25.043-04-03, 6927-MEE-0122, 7146-MEE-0322
FR Base de données publique des médicaments 65565944, 69731801
MT Medicines Authority AA565/32802
MX Comisión Federal para la Protección contra Riesgos Sanitarios 036M82, 037M82
NG Registered Drug Product Database 04-2400, 04-2467
Switch country to Nigeria in order to find specific presentations of ZENTEL
PL Rejestru Produktów Leczniczych 100072539, 100246577, 100292979, 100293654, 100300213, 100300590, 100308924, 100309183, 100324509, 100324685, 100324900, 100326112, 100326170, 100326879, 100330734, 100336820, 100344570, 100346617, 100350369, 100354999, 100355208, 100357555, 100357845, 100358359, 100359985, 100367915, 100369759, 100378037, 100400883, 100419859, 100424040, 100425720, 100436852, 100439081, 100440078, 100454073
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W65214001
SG Health Sciences Authority 05406P, 14030P
ZA Health Products Regulatory Authority 30/12/0354, Q/12/75

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